Canonical Allele Identifier: CA302781762

Gene: CNDP2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.74518403G>A , CM000680.2:g.74518403G>A	GRCh38
NC_000018.9:g.72185638G>A , CM000680.1:g.72185638G>A	GRCh37
NC_000018.8:g.70336618G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324262.9:c.1069-96G>A MANE Select	ENSP00000325548.4:n.1069-96G>A
ENST00000324262.8:c.1069-96G>A	ENSP00000325548.4:n.1069-96G>A
ENST00000324301.12:c.817-96G>A	ENSP00000325756.8:n.817-96G>A
ENST00000577409.1:n.63-96G>A
ENST00000579624.1:c.224-1749G>A	ENSP00000462034.1:n.224-1749G>A
ENST00000579847.5:c.1069-96G>A	ENSP00000462311.1:n.1069-96G>A
ENST00000583695.1:n.500-96G>A
ENST00000584581.5:n.2707G>A
NM_001168499.1:c.817-96G>A	NP_001161971.1:n.817-96G>A
NM_018235.2:c.1069-96G>A	NP_060705.2:n.1069-96G>A
XM_005266728.1:c.1069-96G>A	XP_005266785.1:n.1069-96G>A
XM_006722503.1:c.1069-96G>A	XP_006722566.1:n.1069-96G>A
XM_011526071.1:c.1069-96G>A	XP_011524373.1:n.1069-96G>A
XM_011526072.1:c.1069-96G>A	XP_011524374.1:n.1069-96G>A
XM_011526073.1:c.352-96G>A	XP_011524375.1:n.352-96G>A
XM_005266728.3:c.1069-96G>A	XP_005266785.1:n.1069-96G>A
XM_006722503.2:c.1069-96G>A	XP_006722566.1:n.1069-96G>A
XM_011526072.2:c.1069-96G>A	XP_011524374.1:n.1069-96G>A
XM_011526073.3:c.352-96G>A	XP_011524375.1:n.352-96G>A
NM_018235.3:c.1069-96G>A MANE Select	NP_060705.2:n.1069-96G>A
NM_001370248.1:c.1069-96G>A	NP_001357177.1:n.1069-96G>A
NM_001370249.1:c.1069-96G>A	NP_001357178.1:n.1069-96G>A
NM_001370250.1:c.1069-96G>A	NP_001357179.1:n.1069-96G>A
NM_001370254.1:c.352-96G>A	NP_001357183.1:n.352-96G>A
NM_001168499.2:c.817-96G>A	NP_001161971.1:n.817-96G>A